Gadi IK - Search Results

1

The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13.

Boyd CD, Toth-Fejel SE, Gadi IK, Litt M, Condon MR, Kolbe M, Hagen IK, Kurkinen M, Mackenzie JW, Magenis E. Boyd CD, et al. Among authors: gadi ik. Am J Hum Genet. 1988 Feb;42(2):309-14. Am J Hum Genet. 1988. PMID: 3422542 Free PMC article.

2

High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q.

Bowcock AM, Hebert JM, Wijsman E, Gadi I, Cavalli-Sforza LL, Boyd CD. Bowcock AM, et al. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2701-5. doi: 10.1073/pnas.85.8.2701. Proc Natl Acad Sci U S A. 1988. PMID: 2895928 Free PMC article.

3

Homograft valve durability: host or donor influence?

Gonzalez-Lavin L, Spotnitz AJ, Mackenzie JW, Gu J, Gadi IK, Gullo J, Boyd C, Graf D. Gonzalez-Lavin L, et al. Among authors: gadi ik. Heart Vessels. 1990;5(2):102-6. doi: 10.1007/BF02058326. Heart Vessels. 1990. PMID: 2354984

4

Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review.

Puvabanditsin S, Garrow E, Brandsma E, Savla J, Kunjumon B, Gadi I. Puvabanditsin S, et al. Am J Med Genet A. 2009 Aug;149A(8):1782-5. doi: 10.1002/ajmg.a.32972. Am J Med Genet A. 2009. PMID: 19610110 Review.

5

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG. Burnside RD, et al. Among authors: gadi ik. Hum Genet. 2011 Oct;130(4):517-28. doi: 10.1007/s00439-011-0970-4. Epub 2011 Feb 27. Hum Genet. 2011. PMID: 21359847 Free PMC article.

6

A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies.

Reittinger AM, Helm BM, Boles DJ, Gadi IK, Schrier Vergano SA. Reittinger AM, et al. Among authors: gadi ik. Am J Med Genet A. 2017 Sep;173(9):2528-2533. doi: 10.1002/ajmg.a.38344. Epub 2017 Jun 27. Am J Med Genet A. 2017. PMID: 28653809

7

Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype.

Burnside RD, Pappas JG, Sacharow S, Applegate C, Hamosh A, Gadi IK, Jaswaney V, Keitges E, Phillips KK, Potluri VR, Risheg H, Smith JL, Tepperberg JH, Schwartz S, Papenhausen P. Burnside RD, et al. Among authors: gadi ik. Am J Med Genet A. 2013 Apr;161A(4):822-8. doi: 10.1002/ajmg.a.35699. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495222

8

Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1.

Weisfeld-Adams JD, Edelmann L, Gadi IK, Mehta L. Weisfeld-Adams JD, et al. Among authors: gadi ik. Eur J Med Genet. 2012 Dec;55(12):732-6. doi: 10.1016/j.ejmg.2012.08.011. Epub 2012 Oct 9. Eur J Med Genet. 2012. PMID: 23059467

9

Ovotesticular disorder of sexual development (true hermaphroditism).

Berger-Zaslav AL, Mehta L, Jacob J, Mercado T, Gadi I, Tepperberg JH, Palmer LS. Berger-Zaslav AL, et al. Urology. 2009 Feb;73(2):293-6. doi: 10.1016/j.urology.2008.08.428. Epub 2008 Sep 26. Urology. 2009. PMID: 18822450

10

UPD detection using homozygosity profiling with a SNP genotyping microarray.

Papenhausen P, Schwartz S, Risheg H, Keitges E, Gadi I, Burnside RD, Jaswaney V, Pappas J, Pasion R, Friedman K, Tepperberg J. Papenhausen P, et al. Am J Med Genet A. 2011 Apr;155A(4):757-68. doi: 10.1002/ajmg.a.33939. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21594998

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